ClearanceBrief
510(k) K963320 ยท DQX Wire, Guide, Catheter

TFX MEDICAL GUIDEWIRE

ApplicantTfx Medical Group, Jeffrey NH, US
DecisionSubstantially Equivalent, Dec 3, 1996
ReceivedAug 23, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K963320

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.